Particle size-dependent and surface charge-dependent biodistribution of gold nanoparticles after intravenous administration

作者：Hirn Stephanie; Semmler Behnke Manuela; Schleh Carsten; Wenk Alexander; Lipka Jens; Schaeffler Martin; Takenaka Shinji; Moeller Winfried; Schmid Guenter; Simon Ulrich; Kreyling Wolfgang G^*

来源：European Journal of Pharmaceutics and Biopharmaceutics, 2011, 77(3): 407-416.

DOI：10.1016/j.ejpb.2010.12.029

• Gold nanoparticles
• Intravenous injection
• Female Wistar-Kyoto rat
• In vivo biodistribution
• Nanoparticle size and surface charge
• Hepato-biliary and renal clearance

Gold nanoparticles (GNP) provide many opportunities in imaging, diagnostics, and therapies of nanomedicine. Hence, their biokinetics in the body are prerequisites for specific tailoring of nanomedicinal applications and for a comprehensive risk assessment.
We administered Au-198-radio-labelled monodisperse, negatively charged GNP of five different sizes (1.4, 5, 18, 80, and 200 nm) and 2.8 nm GNP with opposite surface charges by intravenous injection into rats. After 24 h, the biodistribution of the GNP was quantitatively measured by gamma-spectrometry.
The size and surface charge of GNP strongly determine the biodistribution. Most GNP accumulated in the liver increased from 50% of 1.4 nm GNP to >99% of 200 nm GNP. In contrast, there was little size-dependent accumulation of 18-200 nm GNP in most other organs. However, for GNP between 1.4 nm and 5 nm, the accumulation increased sharply with decreasing size: i.e. a linear increase with the volumetric specific surface area. The differently charged 2.8 nm GNP led to significantly different accumulations in several organs.
We conclude that the alterations of accumulation in the various organs and tissues, depending on GNP size and surface charge, are mediated by dynamic protein binding and exchange. A better understanding of these mechanisms will improve drug delivery and dose estimates used in risk assessment.

• 出版日期2011-4